Clinical trial Recruiting at 1 site Interventional Ages 18 to 25 Women only

Group education plus micronutrient supplements to reduce anemia in newly married women in Nepal

Official title: Reducing Anemia Among Young Preconception Women in Nepal Through a Group Household Norm and Micronutrient Supplementation Intervention

Run by University of California, San Francisco · NCT06810440 · Data updated 2026-11-12

This project will try group education with husbands and mothers-in-law plus daily multiple micronutrient supplements to reduce anemia in newly married, non-pregnant women under 25 in Nepal.

More Medication Adherence trials

Quick facts

Study typeInterventional
Ages18 Years to 25 Years
SexWomen only
Enrollment2100 (estimated)
SponsorUniversity of California, San Francisco
Academic / other
Locations1 site (Kathmandu)
StatusRecruiting
StartedOctober 8, 2025
Main results expectedApril 1, 2028
Study endsApril 1, 2029
Registry record updatedMarch 30, 2026
Trial IDNCT06810440 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal participants are newly married women under 25 who are not pregnant, married within the last four months, living with their mother-in-law, willing to participate along with their husband and mother-in-law, and agreeable to blood draws.

Probably not a fit

Women over 25, currently or previously pregnant, married more than four months, not co-residing with a mother-in-law, severely anemic (Hb <8.0 g/dL), unwilling to participate or to have blood drawn, or whose husbands plan to migrate in the next six months are unlikely to benefit or be eligible.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The study pairs the Sumadhur group intervention—educational sessions for newly married women, their husbands, and mothers-in-law—with daily multiple micronutrient supplements (MMS) to improve iron and other nutrient status. It enrolls triads where the woman is under 25, married within the past four months, never pregnant, and co-residing with her mother-in-law, and excludes women with severe anemia (hemoglobin <8.0 g/dL). Hemoglobin is measured by fingerprick Hemocue at enrollment and participants are followed to monitor supplement adherence and changes in micronutrient status. The combined approach aims to shift household norms and practices while providing supplements to increase preconception nutrient stores.

Why it matters

Potential benefit: If successful, this approach could raise preconception hemoglobin and micronutrient levels, reducing maternal anemia and improving pregnancy and newborn outcomes.

How similar studies have gone: Multiple micronutrient supplementation has improved maternal and birth outcomes in other studies, and the Sumadhur group education approach was pilot-tested locally, but combining household norms interventions with MMS at scale remains relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* the newly married couple having been married in the last four months
* women being under 25 years old
* never pregnant and not currently pregnant
* co-residing with the mother-in-law in a household as defined by sharing meals together.
* all triad-household members must also be willing to participate
* husbands must not be planning to migrate in the next 6 months.

Exclusion Criteria:

* Over 25, under 18 years old
* Currently or ever pregnant
* married more than 4 months before
* not co-residing
* not being willing to participate.
* do not consent to blood-draws
* women who are severely anemic (hemoglobin \< 8.0 g/dL) at baseline based on hemoglobin via Hemocue assessment of a fingerprick blood sample at the time of enrollment

Where it's running

  • Center for Research on Environment, Health and Population Activities (CREHPA)
    Kathmandu, Nepal
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.